Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs7130284
rs7130284
1 11 89415204 intron variant C/T snv 0.11 0.800 1.000 1 2013 2013
dbSNP: rs957140
rs957140
1 11 89468459 intron variant G/A snv 0.40 0.800 1.000 1 2013 2013